Variant report

Variant rs956312
Chromosome Location chr4:10188326-10188327
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:10175200-10189000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr4:10181200-10189000 Enhancers HSMM muscle
3 chr4:10183400-10190600 Weak transcription Primary T killer memory cells from peripheral blood blood
4 chr4:10184000-10189200 Weak transcription Right Atrium heart
5 chr4:10184000-10190600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr4:10184000-10194200 Weak transcription HMEC breast
7 chr4:10187000-10188600 Enhancers Right Ventricle heart
8 chr4:10187200-10188400 Enhancers Sigmoid Colon Sigmoid Colon
9 chr4:10187200-10188400 Enhancers NHDF-Ad bronchial
10 chr4:10187200-10188600 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr4:10187400-10188400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr4:10187400-10188600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr4:10187400-10188800 Enhancers HSMMtube muscle
14 chr4:10187400-10189200 Enhancers Left Ventricle heart
15 chr4:10187400-10191800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr4:10187800-10189200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr4:10188200-10188400 Flanking Active TSS Fetal Heart heart
18 chr4:10188200-10190400 Enhancers K562 blood

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